FDA Inspection 1249066 — Randox Laboratories Limited

Randox Laboratories Limited — FEI 3014607865

The FDA completed an inspection of Randox Laboratories Limited on August 8, 2024 in Antrim. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 8, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Antrim (United Kingdom)